Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling-Reference-Cited by-同舟云学术

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Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling

Published:2024-08-31 Issue:1 Volume:14 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Havrylov Serhiy,Chrystal Paul,van Baarle Suey,French Curtis R.,MacDonald Ian M.,Avasarala Jagannadha,Rogers R. Curtis,Berry Fred B.,Kume Tsutomu,Waskiewicz Andrew J.,Lehmann Ordan J.

Funder

Alberta Innovates - Health Solutions

National Sciences and Engineering Research Council of Canada

Canadian Institutes of Health Research

Women and Children's Health Research Institute

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s41598-024-71159-y.pdf

Reference94 articles.

1. Katsanis, N. et al. Triallelic inheritance in Bardet–Biedl syndrome, a Mendelian recessive disorder. Science 293(5538), 2256–2259 (2001).

2. Zaghloul, N. A. et al. Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet–Biedl syndrome. Proc. Natl. Acad. Sci. USA 107(23), 10602–10607 (2010).

3. Huangfu, D. et al. Hedgehog signalling in the mouse requires intraflagellar transport proteins. Nature 426(6962), 83–87 (2003).

4. Schneider, L. et al. PDGFRalphaalpha signaling is regulated through the primary cilium in fibroblasts. Curr. Biol. 15(20), 1861–1866 (2005).

5. Simons, M. et al. Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways. Nat. Genet. 37(5), 537–543 (2005).

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